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PL BioScience ELAREM™ Ultimate-Fdi, Human Platelet Lysate, Fibrinogen-depleted, Viral inactivated
Description
- Virus Inactivated for Highest Safety: The final product is virus-inactivated in order to comply with the guidelines for clinical applications. Virus panel testing is performed according to ICH and EMA guidelines (ICH Q5A (R1) and CPMP/BWP/268/95).
- GMP: The cell culture supplement is tested and released in confirmity with the relevant cGMP guidelines.
- Highly Efficient Cell Performance: Each batch of ELAREM™ Ultimate-FDi is produced from large pools of platelet units to ensure batch-to-batch consistency and enable reproducible conditions.
- No Heparin Addition Required: Due to the fibrinogen-depletion process, ELAREM™ Ultimate-FDi does not require anticoagulant addition. Traces of a xeno-free anticoagulant may be present in the human Platelet Lysate.
- Suited to Cellular Therapeutics: Due to the combination of highest safety standards and efficient cell perfomance, ELAREM™ Ultimate-FDi is suited to clinical trial and therapeutic cell manufacturing needs.
- US Origin: ELAREM™ Ultimate-FDi is a fibrinogen-depleted Human Platelet Lysate of US origin supporting in vitro expansion of various primary cells and cell lines.
- Intended Use: ELAREM™ Ultimate-FDi is for in vitro and manufacturing use only. The product is not intended for direct therapeutic use. For safety precautions, please see appropriate Safety Data Sheet (SDS).
Specifications
Specifications
| Color | Yellow |
| Culture Type | Adherent Cell Culture, Suspension Cell Culture |
| Form | Liquid |
| Product Type | Cell Culture Supplement |
| Sterility | Sterile |
| Sterilization Method | Sterile-filtered |
| Formulation | Liquid, Human Platelet Lysate, Fibrinogen-depleted, Viral-inactivated |
| Purity or Quality Grade | GMP Grade |
| Quantity | 50 mL |
| Shipping Condition | Dry Ice |
Product Title
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